|
ENST00000333646.11:c.4100T>C
|
ENSP00000333125.8:p.Met1367Thr
|
|
|
ENST00000374102.6:c.4220T>C
|
ENSP00000363215.2:p.Met1407Thr
|
|
|
ENST00000685182.1:n.853T>C
|
|
|
|
ENST00000685655.1:c.173T>C
|
ENSP00000509298.1:p.Met58Thr
|
|
|
ENST00000686169.1:n.597T>C
|
|
|
|
ENST00000686548.1:c.*4116T>C
|
ENSP00000509582.1:n.*4116T>C
|
|
|
ENST00000687161.1:n.935T>C
|
|
|
|
ENST00000687382.1:c.4220T>C
|
ENSP00000510724.1:p.Met1407Thr
|
|
|
ENST00000687701.1:n.849T>C
|
|
|
|
ENST00000688079.1:n.2215T>C
|
|
|
|
ENST00000688663.1:c.*1141T>C
|
ENSP00000509348.1:n.*1141T>C
|
|
|
ENST00000688881.1:n.874T>C
|
|
|
|
ENST00000688993.1:n.421T>C
|
|
|
|
ENST00000689768.1:n.2830T>C
|
|
|
|
ENST00000690145.1:c.4220T>C
|
ENSP00000508818.1:p.Met1407Thr
|
|
|
ENST00000690242.1:c.4220T>C
|
ENSP00000510090.1:p.Met1407Thr
|
|
|
ENST00000690250.1:n.1889T>C
|
|
|
|
ENST00000690690.1:c.673T>C
|
|
|
|
ENST00000690828.1:n.4476T>C
|
|
|
|
ENST00000691113.1:c.2699T>C
|
ENSP00000509755.1:n.2699T>C
|
|
|
ENST00000691426.1:n.3349T>C
|
|
|
|
ENST00000691468.1:c.4169T>C
|
ENSP00000509011.1:p.Met1390Thr
|
|
|
ENST00000691909.1:n.940T>C
|
|
|
|
ENST00000692304.1:c.4220T>C
|
ENSP00000508427.1:p.Met1407Thr
|
|
|
ENST00000692893.1:n.1529T>C
|
|
|
|
ENST00000692964.1:n.884T>C
|
|
|
|
ENST00000693050.1:n.727T>C
|
|
|
|
ENST00000693324.1:c.4184T>C
|
ENSP00000508643.1:p.Met1395Thr
|
|
|
ENST00000693391.1:c.2165T>C
|
ENSP00000509563.1:p.Met722Thr
|
|
|
ENST00000374080.8:c.4220T>C
MANE Select
|
ENSP00000363193.3:p.Met1407Thr
|
|
|
ENST00000333646.10:c.3761T>C
|
ENSP00000333125.7:p.Met1254Thr
|
|
|
ENST00000374080.7:c.4220T>C
|
ENSP00000363193.3:p.Met1407Thr
|
|
|
ENST00000374102.5:c.4220T>C
|
ENSP00000363215.1:p.Met1407Thr
|
|
|
NM_005120.2:c.4220T>C
|
NP_005111.2:p.Met1407Thr
|
|
|
XM_005262317.1:c.4220T>C
|
XP_005262374.1:p.Met1407Thr
|
|
|
XM_005262319.1:c.4220T>C
|
XP_005262376.1:p.Met1407Thr
|
|
|
NM_005120.3:c.4220T>C
MANE Select
|
NP_005111.2:p.Met1407Thr
|
|
